Home NDC 43742-1509 Gum Therapy
Product NDC 43742-1509
11-digit product format 437421509
Labeler code 43742
Product ID 43742-1509_d9c12636-2f2a-4677-94e9-eb2c33768804
Type HUMAN OTC DRUG
Nonproprietary name Calendula Officinalis, Kali Phosphoricum, Natrum Muriaticum, Arnica Montana, Agave Americana, Cistus Canadensis, Kreosotum, Myrrha, Calcarea Fluorica, Aconitum Napellus, Bismuthum Subnitricum, Sepia, Hepar Sulphuris Calcareum, Mercurius Vivus
Dosage form LIQUID
Route ORAL
Labeler Deseret Biologicals
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-08-20
Marketing end 2027-04-25
Substance ACONITUM NAPELLUS; AGAVE AMERICANA LEAF; ARNICA MONTANA; BISMUTH SUBNITRATE; CALCIUM FLUORIDE; CALCIUM SULFIDE; CALENDULA OFFICINALIS FLOWERING TOP; DIBASIC POTASSIUM PHOSPHATE; HELIANTHEMUM CANADENSE; MERCURY; MYRRH; SEPIA OFFICINALIS JUICE; SODIUM CHLORIDE; WOOD CREOSOTE
Active strength 12; 6; 6; 12; 12; 12; 1; 3; 6; 12; 8; 12; 3; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Bismuth [CS], Bismuth [EPC]
NDC exclude flag No
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Gum Therapy Active Ingredients# Ingredient, Strength table Ingredient Strength CALENDULA OFFICINALIS FLOWERING TOP 12 [hp_X]/mL DIBASIC POTASSIUM PHOSPHATE 6 [hp_X]/mL SODIUM CHLORIDE 6 [hp_X]/mL ARNICA MONTANA 12 [hp_X]/mL AGAVE AMERICANA LEAF 12 [hp_X]/mL HELIANTHEMUM CANADENSE 12 [hp_X]/mL WOOD CREOSOTE 1 [hp_X]/mL MYRRH 3 [hp_X]/mL CALCIUM FLUORIDE 6 [hp_X]/mL ACONITUM NAPELLUS 12 [hp_X]/mL BISMUTH SUBNITRATE 8 [hp_X]/mL SEPIA OFFICINALIS JUICE 12 [hp_X]/mL CALCIUM SULFIDE 3 [hp_X]/mL MERCURY 6 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 14 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43742-1509-1 Gum Therapy 30 mL in 1 BOTTLE, DROPPER LIQUID 30 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43742-1509 GUM THERAPY (CALENDULA OFFICINALIS, KALI PHOSPHORICUM, NATRUM MURIATICUM, ARNICA MONTANA, AGAVE AMERICANA, CISTUS CANADENSIS, KREOSOTUM, MYRRHA, CALCAREA FLUORICA, ACONITUM NAPELLUS, BISMUTHUM SUBNITRICUM, SEPIA, HEPAR SULPHURIS CALCAREUM, MERCURIUS VIVUS) LIQUID [DESERET BIOLOGICALS] 4 Current NDC, Legacy NDC, 1 package rows 20230720_0cf8a815-808d-4018-baf9-2b4545fc7ea8.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Gum Therapy CALENDULA OFFICINALIS, KALI PHOSPHORICUM, NATRUM MURIATICUM, ARNICA MONTANA, AGAVE AMERICANA, CISTUS CANADENSIS, KREOSOTUM, MYRRHA, CALCAREA FLUORICA, ACONITUM NAPELLUS, BISMUTHUM SUBNITRICUM, SEPIA, HEPAR SULPHURIS CALCAREUM, MERCURIUS VIVUS Deseret Biologicals 0cf8a815-808d-4018-baf9-2b4545fc7ea8 2023-07-19 Warnings Exact identifier ndc (product): 43742-1509
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43742-1509-1 43742150901 30 mL in 1 BOTTLE, DROPPER (43742-1509-1) 30 ml 2019-08-20 2027-04-25 No No Current